Institute for Cardiovascular and Metabolic Research, School of Biological Sciences, University of Reading, Whiteknights, Reading RG6 6UB, UK.
Cell Signal. 2011 Feb;23(2):468-77. doi: 10.1016/j.cellsig.2010.10.024. Epub 2010 Oct 30.
ERK1 and ERK2 (ERK1/2) are central to the regulation of cell division, growth and survival. They are activated by phosphorylation of the Thr- and the Tyr- residues in their Thr-Glu-Tyr activation loops. The dogma is that dually-phosphorylated ERK1/2 constitute the principal activities in intact cells. We previously showed that, in neonatal rat cardiac myocytes, endothelin-1 and phorbol 12-myristate 13-acetate (PMA) powerfully and rapidly (maximal at ~5 min) activate ERK1/2. Here, we show that dually-phosphorylated ERK1/2 rapidly (< 2 min) appear in the nucleus following stimulation with endothelin-1. We characterized the active ERK1/2 species in myocytes exposed to endothelin-1 or PMA using MonoQ FPLC. Unexpectedly, two peaks of ERK1 and two peaks of ERK2 activity were resolved using in vitro kinase assays. One of each of these represented the dually-phosphorylated species. The other two represented activities for ERK1 or ERK2 which were phosphorylated solely on the Thr- residue. Monophosphothreonyl ERK1/2 represented maximally ~30% of total ERK1/2 activity after stimulation with endothelin-1 or PMA, and their k(cat) values were estimated to be minimally ~30% of the dually-phosphorylated species. Appearance of monophosphothreonyl ERK1/2 was rapid but delayed in comparison with dually-phosphorylated ERK1/2. Of 10 agonists studied, endothelin-1 and PMA were most effective in terms of ERK1/2 activation and in stimulating the appearance of monophosphothreonyl and dually-phosphorylated ERK1/2. Thus, enzymically active monophosphothreonyl ERK1/2 are formed endogenously following activation of the ERK1/2 cascade and we suggest that monophosphothreonyl ERK1/2 arise by protein tyrosine phosphatase-mediated dephosphorylation of dually-phosphorylated ERK1/2.
ERK1 和 ERK2(ERK1/2)是细胞分裂、生长和存活调节的核心。它们通过 Thr 和 Tyr 残基在其 Thr-Glu-Tyr 激活环中的磷酸化而被激活。传统观点认为,双磷酸化的 ERK1/2 构成完整细胞中的主要活性。我们之前表明,在内质皮素-1 和佛波醇 12-肉豆蔻酸 13-乙酸酯(PMA)刺激下,新生大鼠心肌细胞中 ERK1/2 迅速而强烈地激活(最大在5 分钟)。在这里,我们表明,在受到内皮素-1 刺激后,双磷酸化的 ERK1/2 迅速(<2 分钟)出现在细胞核中。我们使用 MonoQ FPLC 对暴露于内皮素-1 或 PMA 的心肌细胞中的活性 ERK1/2 进行了特征描述。出乎意料的是,使用体外激酶测定法可分辨 ERK1 和 ERK2 的两个活性峰。其中一个代表双磷酸化的物种。另外两个代表仅在 Thr-残基上磷酸化的 ERK1 或 ERK2 的活性。在受到内皮素-1 或 PMA 刺激后,磷酸化的 Thr-残基的 ERK1/2 代表了最大30%的总 ERK1/2 活性,其 k(cat) 值估计为双磷酸化物种的最小~30%。与双磷酸化的 ERK1/2 相比,磷酸化的 Thr-残基的 ERK1/2 的出现速度较快,但延迟。在所研究的 10 种激动剂中,内皮素-1 和 PMA 在 ERK1/2 激活和刺激磷酸化的 Thr-残基的 ERK1/2 和双磷酸化的 ERK1/2 的出现方面最为有效。因此,ERK1/2 级联激活后,内源性形成具有酶活性的磷酸化 Thr-残基的 ERK1/2,我们认为磷酸化 Thr-残基的 ERK1/2 是通过蛋白酪氨酸磷酸酶介导的双磷酸化的 ERK1/2 去磷酸化形成的。